Recall record at a glance
| Official record | F-1823-2018 |
|---|---|
| Category | Food Recalls |
| Classification | Class III |
| FDA record status | Terminated |
| Recalling firm | Severino Pasta Manufacturing, Inc. |
| Report date | Aug 22, 2018 |
| Recall initiation date | Jul 25, 2018 |
| Quantity | 42 cases, 378 units were produced |
| Location | Westmont, NJ, United States |
Official product description
Severino Home Made, Artisanal Small Batch Pasta, Raviolini Cheese, 9 units x 9 oz per case. Expiration March 2019.
Why the product was recalled
Severino Pasta Manufacturing, Inc. has initiated a recall of their Severino Pasta Super Fresh Cheese Raviolini due to undeclared eggs. The retail unit has the correct label on top, Cheese Raviolini which declares the precense of eggs in the ingredient statement and contains statement. However, the product has the incorrect label on the bottom, Cheese Rigatoni, which does not declare eggs in the ingredient statement or contains statement. The Raviolini label declares: Wheat, Milk, and Eggs whereas the Rigatoni label declares: Wheat and Milk. Since both labels are on the product consumers may be confused as to which ingredients are actually present.
Distribution information
Product was distributed to Whole Foods Markets in the Florida and the NE/NA Region (Massachusetts, Connecticut, Rhode Island, New Hampshire, Maine) Whole Foods Florida DC, 2700 NW 19th Street, Ste 100, Pompano Beach, FL. Whole Foods NE/NA DC, 400 East Johnson Ave, Cheshire, CT. 06410
How to read the classification
FDA Class III generally covers situations in which use of or exposure to the product is not likely to cause adverse health consequences. The classification displayed here is taken from the FDA enforcement record.
Additional record details
Recall type: Voluntary: Firm initiated. Initial notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.
What to do next
If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.
About this record
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